Product NDC: | 50789-436 |
Proprietary Name: | Oxygen |
Non Proprietary Name: | Oxygen |
Active Ingredient(s): | 930 mL/L & nbsp; Oxygen |
Administration Route(s): | RESPIRATORY (INHALATION) |
Dosage Form(s): | GAS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50789-436 |
Labeler Name: | Maniilaq Association |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED MEDICAL GAS |
Start Marketing Date: | 20120101 |
Package NDC: | 50789-436-03 |
Package Description: | 400 L in 1 CYLINDER (50789-436-03) |
NDC Code | 50789-436-03 |
Proprietary Name | Oxygen |
Package Description | 400 L in 1 CYLINDER (50789-436-03) |
Product NDC | 50789-436 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Oxygen |
Dosage Form Name | GAS |
Route Name | RESPIRATORY (INHALATION) |
Start Marketing Date | 20120101 |
Marketing Category Name | UNAPPROVED MEDICAL GAS |
Labeler Name | Maniilaq Association |
Substance Name | OXYGEN |
Strength Number | 930 |
Strength Unit | mL/L |
Pharmaceutical Classes |